Home
>
National Drug Code (NDC)
>
Rembrandt Canker Sore
Rembrandt Canker Sore - 42002-441-03 - (Sodium Fluoride)
Drug Information of Rembrandt Canker Sore
| Product NDC: | 42002-441 |
| Proprietary Name: | Rembrandt Canker Sore |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 2.43 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rembrandt Canker Sore
| Product NDC: | 42002-441 |
| Labeler Name: | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120316 |
Package Information of Rembrandt Canker Sore
| Package NDC: | 42002-441-03 |
| Package Description: | 1 TUBE in 1 CARTON (42002-441-03) > 85 g in 1 TUBE |
NDC Information of Rembrandt Canker Sore
| NDC Code | 42002-441-03 |
| Proprietary Name | Rembrandt Canker Sore |
| Package Description | 1 TUBE in 1 CARTON (42002-441-03) > 85 g in 1 TUBE |
| Product NDC | 42002-441 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | ORAL |
| Start Marketing Date | 20120316 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.43 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
